Last synced on 20 December 2024 at 11:05 pm

Reagents, Zika Virus Nucleic Acid

Page Type
Product Code
Definition
Nucleic acid-based in vitro diagnostic devices for the detection of Zika virus and diagnosis of Zika virus infection in human clinical specimens.
Physical State
In Vitro Diagnostic Primers, Probes and/or capture oligonucleotides.
Technical Method
Nucleic acid amplification.
Target Area
The device is an in-vitro diagnostic device; none of the body parts will utilize the device or are intended to be affected by the device.
Review Panel
Microbiology
Submission Type
EUA - Emergency Use Authorization
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code POA is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.

Reagents, Zika Virus Nucleic Acid

Page Type
Product Code
Definition
Nucleic acid-based in vitro diagnostic devices for the detection of Zika virus and diagnosis of Zika virus infection in human clinical specimens.
Physical State
In Vitro Diagnostic Primers, Probes and/or capture oligonucleotides.
Technical Method
Nucleic acid amplification.
Target Area
The device is an in-vitro diagnostic device; none of the body parts will utilize the device or are intended to be affected by the device.
Review Panel
Microbiology
Submission Type
EUA - Emergency Use Authorization
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code POA is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.